Daniel H. Geschwind
Program in Neurogenetics
Department of Neurology
and the Center for Neurobehavioral Genetics
Neuropsychiatric Institute
USA
Name/email consistency: high
- Neuroscience in the era of functional genomics and systems biology. Geschwind, D.H., Konopka, G. Nature (2009)
- Autism: the ups and downs of neuroligin. Geschwind, D.H. Biol. Psychiatry (2009)
- Autism: many genes, common pathways?. Geschwind, D.H. Cell (2008)
- Autism spectrum disorders: developmental disconnection syndromes. Geschwind, D.H., Levitt, P. Curr. Opin. Neurobiol. (2007)
- Autism: searching for coherence. Geschwind, D. Biol. Psychiatry (2007)
- GENSAT: a genomic resource for neuroscience research. Geschwind, D. Lancet. Neurol (2004)
- DNA microarrays: translation of the genome from laboratory to clinic. Geschwind, D.H. Lancet. Neurol (2003)
- Tau phosphorylation, tangles, and neurodegeneration: the chicken or the egg?. Geschwind, D.H. Neuron (2003)
- Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness. Geschwind, D.H., Miller, B.L., DeCarli, C., Carmelli, D. Proc. Natl. Acad. Sci. U.S.A. (2002)
- A genetic analysis of neural progenitor differentiation. Geschwind, D.H., Ou, J., Easterday, M.C., Dougherty, J.D., Jackson, R.L., Chen, Z., Antoine, H., Terskikh, A., Weissman, I.L., Nelson, S.F., Kornblum, H.I. Neuron (2001)
- Sharing gene expression data: an array of options. Geschwind, D.H. Nat. Rev. Neurosci. (2001)
- Molecular approaches to cerebral laterality: development and neurodegeneration. Geschwind, D.H., Miller, B.L. Am. J. Med. Genet. (2001)
- Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia. Geschwind, D.H., Robidoux, J., Alarcón, M., Miller, B.L., Wilhelmsen, K.C., Cummings, J.L., Nasreddine, Z.S. Ann. Neurol. (2001)
- Neurobehavioral phenotype of Klinefelter syndrome. Geschwind, D.H., Boone, K.B., Miller, B.L., Swerdloff, R.S. Ment. Retard. Dev. Disabil. Res. Rev (2000)
- Mice, microarrays, and the genetic diversity of the brain. Geschwind, D.H. Proc. Natl. Acad. Sci. U.S.A. (2000)
- Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Geschwind, D.H., Loginov, M., Stern, J.M. Am. J. Hum. Genet. (1999)
- Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray. Geschwind, D.H., Gregg, J., Boone, K., Karrim, J., Pawlikowska-Haddal, A., Rao, E., Ellison, J., Ciccodicola, A., D'Urso, M., Woods, R., Rappold, G.A., Swerdloff, R., Nelson, S.F. Dev. Genet. (1998)
- The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. Geschwind, D.H., Perlman, S., Figueroa, C.P., Treiman, L.J., Pulst, S.M. Am. J. Hum. Genet. (1997)
- Identification and characterization of novel developmentally regulated proteins in rat spinal cord. Geschwind, D.H., Kelly, G.M., Fryer, H., Feeser-Bhatt, H., Hockfield, S. Brain Res. Dev. Brain Res. (1996)